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首页> 外文期刊>Current cancer drug targets >Disulfiram, and disulfiram derivatives as novel potential anticancer drugs targeting the ubiquitin-proteasome system in both preclinical and clinical studies.
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Disulfiram, and disulfiram derivatives as novel potential anticancer drugs targeting the ubiquitin-proteasome system in both preclinical and clinical studies.

机译:在临床前和临床研究中,双硫仑和双硫仑衍生物作为靶向泛素-蛋白酶体系统的新型潜在抗癌药物。

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摘要

Disulfiram is a FDA approved drug for the treatment of alcoholism and available for clinical use since over 5 decades. Despite data from the 1970s and 80s that showed that disulfiram and analogs are able to enhance the activity of anticancer cytotoxic drugs and might be useful chemopreventative agents, the underlying molecular mechanisms remained unknown until recently. Large scale screening efforts for agents that can inhibit the proteasome and be used as novel anticancer drugs, revealed that disulfiram has proteasome inhibitory activity. Moreover, disulfiram was also found to have specific activity against zinc fingers and RING-finger ubiquitin E3 ligases that play an important role in cancer development. Here, we review the preclinical and clinical studies exploring disulfiram as an anticancer agent as well as research programs that focus on the development of disulfiram derivatives as inhibitors of the ubiquitin-proteasome system.
机译:Disulfiram是FDA批准的用于治疗酒精中毒的药物,自5年来已有临床应用。尽管从1970年代和80年代的数据表明双硫仑和类似物能够增强抗癌细胞毒性药物的活性,并且可能是有用的化学预防剂,但直到最近,其潜在的分子机制仍然未知。对可以抑制蛋白酶体并被用作新型抗癌药的药物的大规模筛选工作表明,双硫仑具有蛋白酶体抑制活性。此外,还发现双硫仑具有针对锌指和RING指泛素E3连接酶的特异性活性,而锌指和RING指泛素E3连接酶在癌症的发展中起着重要的作用。在这里,我们回顾了探讨双硫仑作为抗癌剂的临床前和临床研究,以及着重于开发作为泛素-蛋白酶体系统抑制剂的双硫仑衍生物的研究计划。

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